KINETICREAM PAIN RELIEVING TOPICAL ANALGESIC- menthol cream

Drug Labeling and Warnings

Drug Details [pdf]

Drug Facts

Active Ingredient

Menthol 2.00%

Purpose

External Analgesic

Uses:

For temporary relief of minor aches and pains associated with backache, muscle ache, joint pain, arthritis, bruises and sprains.

Warnings:

• For external use only.
• Avoid contact with eyes.
• Do not apply to open wounds or damaged skin.
• If symptoms persist for more than seven days, discontinue use and consult physician.

Keep out of reach of children.

• If swallowed, consult physician.
• Do not bandage tightly.

If pregnant or breast feeding,

consult physician prior to use.

Directions.

Shake well prior to using. Apply to area of discomfort. Smooth out and allow to absorb into skin. Do not use more than four times per day.Do not use near eyes. For best results, use immediately after showering.

Inactive Ingredients:

Aloe Barbadensis Leaf (Aloe Vera Juice) Gel, Aqua (Deionized Water), Arnica Montrana Flower Extract, Bromelain, Butyrospermum Parkii (Shea) Butter, C13-14 lsoparaffin, Calophyllum Tacamahaca (Tamanu) Oil, Camellia Sinensis Leaf (Green Tea) Extract, Cetearyl Alcohol, Cetyl Myristoleate, Chondroitin Sulfate, Citric Acid, Citrus Aurantium Bergamia (Bergamot) Oil, Dimethyl Sulfone (MSM), Emu Oil, Ethylhexylglycerin, Glycerin, Glucosamine Sulfate, Glyceryl Stearate SE, Laureth-7, Melia Azadirachta (Neem) Seed Oil, Mentha Piperita (Peppermint) Oil, Papain, Phenoxyethanol, Polyacrylamide, Polysorbate-20, Salix Alba (Willow Bark) Extract, SD-Alcohol 40B, Sesamum lndicum (Sesame) Oil, Stearic Acid, Theobroma Cacao (Cocoa) Seed Butter, Tocopheryl Acetate (Vitamin-E), Xanthan Gum.

Questions or Comments?

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Package Labeling:

INGREDIENTS AND APPEARANCE

KINETICREAM PAIN RELIEVING TOPICAL ANALGESIC 
menthol cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 58611-971
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A)	MENTHOL	20 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
ALOE VERA LEAF (UNII: ZY81Z83H0X)
WATER (UNII: 059QF0KO0R)
ARNICA MONTANA FLOWER (UNII: OZ0E5Y15PZ)
BROMELAIN (UNII: U182GP2CF3)
SHEA BUTTER (UNII: K49155WL9Y)
C13-14 ISOPARAFFIN (UNII: E4F12ROE70)
TAMANU OIL (UNII: JT3LVK84A1)
GREEN TEA LEAF (UNII: W2ZU1RY8B0)
CETEARYL ALCOHOL (UNII: 2DMT128M1S)
CETYL MYRISTOLEATE (UNII: 87P8K33Q5X)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
BERGAMOT OIL (UNII: 39W1PKE3JI)
DIMETHYL SULFONE (UNII: 9H4PO4Z4FT)
EMU OIL (UNII: 344821WD61)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
GLYCERIN (UNII: PDC6A3C0OX)
GLUCOSAMINE SULFATE (UNII: 1FW7WLR731)
GLYCERYL STEARATE SE (UNII: FCZ5MH785I)
LAURETH-7 (UNII: Z95S6G8201)
AZADIRACHTA INDICA SEED OIL (UNII: 4DKJ9B3K2T)
PEPPERMINT OIL (UNII: AV092KU4JH)
PAPAIN (UNII: A236A06Y32)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
POLYSORBATE 20 (UNII: 7T1F30V5YH)
SALIX ALBA BARK (UNII: 205MXS71H7)
SESAME OIL (UNII: QX10HYY4QV)
STEARIC ACID (UNII: 4ELV7Z65AP)
COCOA BUTTER (UNII: 512OYT1CRR)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
XANTHAN GUM (UNII: TTV12P4NEE)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 58611-971-00	101 mL in 1 BOTTLE; Type 0: Not a Combination Product	02/02/2026

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M017	02/02/2026

Labeler - Phoenix Bioperformance Products LLC (034681162)

Registrant - Pure Source, LLC (080354456)